Nailfold capillaroscopy by smartphone-dermatoscope for connective tissue disease diagnosis in interstitial lung disease: a prospective observational study

Autor: Adelle S. Jee, Matthew J.S. Parker, Neil McGill, Jane F. Bleasel, Susanne Webster, Lauren K. Troy, Tamera J. Corte

Publikováno v: ERJ Open Research, Vol 7, Iss 4 (2021)

Nailfold capillaroscopy (NFC) is a non-invasive tool validated for systemic sclerosis diagnosis. The role and interpretation of NFC in interstitial lung disease (ILD) patients for the diagnosis of connective tissue disease associated ILD (CTD-ILD) re

Externí odkaz: https://doaj.org/article/8642c72f3fa74ec0a7fdcd5260763726

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Diagnosis and management of connective tissue disease‐associated interstitial lung disease in Australia and New Zealand: A position statement from the Thoracic Society of Australia and New Zealand*

Autor: Jeremy P. Wrobel, Adelle S. Jee, Ian Glaspole, Leona M. Dowman, Lauren K. Troy, Lissa Spencer, Helen E. Jo, Sally Chapman, Tamera J. Corte, Anne E Holland, Sally de Boer, Nicole S L Goh, Daniel C. Chambers, Taryn Reddy, Jane Bleasel, Matthew J.S. Parker, Peter Hopkins, Paul N. Reynolds, Yuben Moodley, Karen Symons, Margaret L. Wilsher, Robert Sheehy, Gregory J Keir, Christopher Grainge

Publikováno v: Respirology (Carlton, Vic.)

© 2020 The Authors. Respirology published by John Wiley & Sons Australia, Ltd on behalf of Asian Pacific Society of Respirology. Pulmonary complications in CTD are common and can involve the interstitium, airways, pleura and pulmonary vasculature. I

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aada05cd49f3034d8fa8ea1ddd07aed4
http://europepmc.org/articles/PMC7894187

Adult idiopathic inflammatory myopathies

Autor: James B. Lilleker, Matthew J.S. Parker, Hector Chinoy

Publikováno v: Parker, M JS, Lilleker, J & Chinoy, H 2021, ' Adult idiopathic inflammatory myopathies ', Medicine
. https://doi.org/10.1016/j.mpmed.2021.10.011

The idiopathic inflammatory myopathies represent a rare group of diseases characterized by autoimmune inflammation of skeletal muscle and other organs. There has been significant recent progress in understanding pathogenesis, phenotyping disease subt

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::908945f783840c2dd0fe864cb2ab5545
https://pure.manchester.ac.uk/ws/files/204278338/50_1Chinoy_et_al_changes_accepted.docx

Polymyositis:is there anything left? A retrospective diagnostic review from a tertiary myositis centre

Autor: Matthew J.S. Parker, Jesús Loarce-Martos, James B. Lilleker, Neil McHugh, Hector Chinoy

Publikováno v: Loarce-Martos, J, Lilleker, J B, Parker, M, McHugh, N & Chinoy, H 2021, ' Polymyositis : is there anything left? A retrospective diagnostic review from a tertiary myositis centre ', Rheumatology (Oxford, England), vol. 60, no. 7, pp. 3398–3403 . https://doi.org/10.1093/rheumatology/keaa801
Loarce-Martos, J, Lilleker, J B, Parker, M, McHugh, N & Chinoy, H 2021, ' Polymyositis: is there anything left? A retrospective diagnostic review from a tertiary myositis centre ', Rheumatology, vol. 60, no. 7, pp. 3398-3403 . https://doi.org/10.1093/rheumatology/keaa801

Objective The current classification criteria for idiopathic inflammatory myopathy (IIM) retain PM as a major disease subgroup. However, evolution in the understanding of IIM has suggested that many of these patients could be better described as havi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d70ffe16e7e5afdb5538d19c04584eca
https://purehost.bath.ac.uk/ws/files/217512987/PM_Rheumatology_08_11_clean.pdf